TRAZODONE HYDROCHLORIDE
- Product NDC
- 61919-631
- 11-digit product format
- 619190631
- Labeler code
- 61919
- Product ID
- 61919-631_e9d112d7-6f63-05a7-e053-2a95a90a7730
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TRAZODONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA205253
- Marketing category
- ANDA
- Marketing start
- 2019-08-19
- Marketing end
- 0000-00-00
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6E8ZO8LRNM | TRAZODONE HYDROCHLORIDE | 25332-39-2 | TRAZODONE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-631-30 | 61919063130 | 30 TABLET in 1 BOTTLE (61919-631-30) | 30 tablet | 2019-08-19 | 0000-00-00 | No | No | Current |
| 61919-631-60 | 61919063160 | 60 TABLET in 1 BOTTLE (61919-631-60) | 60 tablet | 2019-08-19 | 0000-00-00 | No | No | Current |
| 61919-631-90 | 61919063190 | 90 TABLET in 1 BOTTLE (61919-631-90) | 90 tablet | 2019-08-19 | 0000-00-00 | No | No | Current |